Claims for Patent: 9,663,792

Summary for Patent: 9,663,792

Title:	Plant mitochondria transformation method
Abstract:	Method for heterologous RNA species and protein production in plant cell mitochondria comprising introducing into plant cells nucleic acid components that encode heterologous proteins/RNAS under the control of promoters operative in mitochondria, vectors, host cells, plants and uses thereof.
Inventor(s):	Malcuit; Isabelle (London, GB), Sorokin; Alexander (London, GB)
Assignee:	Algentech SAS (Envry, FR)
Application Number:	13/131,081
Patent Claims:	1. A method of transforming a plant cell, the method comprising: 1) introducing into the plant cell a first nucleic acid sequence that comprises a plant nuclear promoter operably linked to a first nucleic acid sequence that comprises a plant mitochondrion transgene cassette, a plant mitochondrion translocation sequence from a group II intron RNA, wherein the group II intron is Ll.LtrB, and a primer binding domain; and 2) introducing into the plant cell a second nucleic acid sequence that encodes for a translocation sequence binding protein from an intron encoded protein (IEP) of a group II intron, wherein the IEP is LtrA fused to a plant mitochondrion transit peptide, wherein the second nucleic acid sequence is operably linked to a plant nuclear promoter, and wherein the mitochondrion translocation sequence of the product of 1) binds with the translocation sequence binding protein of the product of 2). 2. The method according to claim 1, wherein the plant mitochondrion transgene cassette comprises: i) a left flanking sequence (LFS) having least one mitochondrion specific promoter (mPRO) and a right flanking sequence (RFS) having at least one mitochondrion specific terminator (mTER) sequence; and ii) at least one isolated nucleic acid of interest. 3. The method according to claim 1, wherein the said isolated nucleic acid sequence is a recombinant DNA sequence or an introduced native, isolated genomic DNA sequence selected from isolated mammalian or plant nucleic acid sequences. 4. The method according to claim 3, wherein the isolated nucleic acid sequence is selected from nucleic acid sequences encoding proteins that confer cytoplasmic male sterility to a plant. 5. The method according to claim 1, wherein the primer binding domain is selected from that of a retrotransposon, or of a retrovirus. 6. A method of producing at least a heterologous or exogenous RNA species in a plant that comprises: 1) introducing into a regenerable plant cell a nucleic acid sequence that comprises a plant nuclear promoter operably linked to a first nucleic acid sequence that comprises a plant mitochondrion transgene cassette, a plant mitochondrion translocation sequence from a group II intron RNA, wherein the group II intron is Ll.LtrB, and a primer binding domain; 2) introducing into the regenerable plant cell a second nucleic acid sequence that encodes for a translocation sequence binding protein from an intron encoded protein (IEP) of a group II intron, wherein the IEP is LtrA fused to a plant mitochondrion transit peptide, and wherein said second nucleic acid sequence is operably linked to a plant nuclear promoter; 3) growing the regenerable plant cell of steps 1) to 2); 4) selecting a plant cell of 3), wherein the transgene comprised within the plant mitochondrion transgene cassette is integrated into the mitochondrial genome; 5) regenerating a plant from the plant cell of 4); and 6) growing the plant of 5). 7. The method according to claim 6, wherein the heterologous or exogenous RNA species encoded by the transgene that is integrated into the mitochondrion is expressed as a heterologous or exogenous protein. 8. An isolated polynucleotide sequence that comprises a plant nuclear promoter operably linked to a first nucleic acid sequence that comprises a plant mitochondrion transgene cassette, a plant mitochondrion translocation sequence from a group II intron RNA, wherein the group II intron is Ll.LtrB, and a primer binding domain for use in a method according to claim 1. 9. An isolated polynucleotide sequence that encodes for a mitochondrion translocation sequence-binding protein fused to a plant mitochondrion transit peptide wherein the polynucleotide sequence is operably linked to a plant nuclear promoter for use in a method according to claim 1. 10. An isolated polynucleotide sequence that encodes for a mitochondrion translocation sequence-binding protein from an intron encoded protein (IEP) of a group II intron, wherein the IEP is LtrA fused to a plant mitochondrion transit peptide, and wherein the polynucleotide sequence is operably linked to a plant nuclear promoter for use in a method according to claim 6. 11. An isolated polynucleotide sequence that encodes for a reverse transcriptase protein fused to a plant mitochondrion transit peptide, wherein the polynucleotide sequence is operably linked to a plant nuclear promoter for use in a method according to claim 1. 12. An isolated polynucleotide sequence that encodes for a reverse transcriptase protein fused to a plant mitochondrion transit peptide wherein the polynucleotide sequence is operably linked to a plant nuclear promoter for use in a method according to claim 6. 13. The isolated polynucleotide sequence according to claim 8 comprising genomic DNA or cDNA. 14. A cell containing a heterologous polynucleotide according to claim 8 comprised in a plant, a plant part, or a plant propagule, or in plant cell culture wherein the plant is selected from the group consisting of tobacco (Nicotiana tabacum) and other Nicotiana species, carrot, vegetable and oilseed Brassicas, melons, capsicums, grape vines, lettuce, strawberry, sugar beet, wheat, barley, corn (maize), rice, peas, sorghum, sunflower, tomato, cotton, and potato. 15. The method according to claim 3, wherein the isolated nucleic acid sequence is selected from nucleic acid sequences encoding proteins selected from the petunia mitochondrion pcf sequence, the orf107 sequence of sorghum and the orf79 of rice. 16. The method according to claim 1, wherein the primer binding domain is selected from the yeast Ty1 retrotransposon and the TnT1 tobacco retrotransposon. 17. The method according to claim 1, wherein the MTS sequence is selected from the group II intron-derived MTS from the Lactococcus lactis Ll.LtrB intron.

Details for Patent 9,663,792

Applicant	Tradename	Biologic Ingredient	Dosage Form	BLA	Approval Date	Patent No.	Expiredate
Merck Sharp & Dohme Corp.	INTRON A	interferon alfa-2b	For Injection	103132	06/04/1986		2028-11-25
Merck Sharp & Dohme Corp.	INTRON A	interferon alfa-2b	For Injection	103132			2028-11-25
Merck Sharp & Dohme Corp.	INTRON A	interferon alfa-2b	Injection	103132			2028-11-25